"""•To ensure compliance of procedure and practices in line with GMP guidelines and regulatory expectations for concerned manufacturing facilities and products of Biotech division, Cadila Pharmaceuticals Ltd. . •Review and release of Batche...
Follow cGMP and GLP PRACTICES. • To ensure current good laboratory compliance and ensuring all SOPs related to Quality Control laboratory are prepared and reviewed / implemented properly. • To follow safety Procedure in QC department. • To ...
"• To ensure operation and maintenance of Electrical network (HT & LT) of plant as well as planning, designing ordering & execution of brown field electrical project. • Ensure compliance to cGMP requirements & Good Engineering Practice requ...
To perform In-process Quality Assurance for the process / products being manufactured and packed in Main Pharma Block (Tablet / Capsule). To ensure Quality and cGMP compliance of the products being manufactured and Packed in Main Pharma Blo...
"• To meet agreed production targets with due compliance to regulatory norms. • To ensure proper utilization and productivity of manpower and machines. • To ensure all records/documents of department are maintained in compliance to regulato...
- To develop chemical process which is having least hazardous chemicals and cost effective process of API in lab and the technology to be transferred at plant scale. - To check the proof of concept of selected synthetic route. - To develop ...
· To ensure Registration dossier submission of products in different Africa countries (Region I) as per agreed timeline. · To ensure Renewal of registered product prior to validity expiration of Africa countries (Region I). · To Review Regi...
Responsibility - Lab demonstration & scale up of new DMF and NDMF molecules, Process Optimization before Scale-up activities, Execution of Kilo Lab batches & technology transfer activity. Principal Tasks and Responsibilities: - Understandin...
- Analytical method development as per ICH guideline for OSD and injectable dosage form - Perform analytical method validation / verification as per the protocol. - To perform routine and stability sample analysis. - Analytical method trans...
Major Purpose of the Job: - To develop a synthetic process for DMF and non-DMF molecules (API) as allotted. - To perform experiments in lab as per Planning given by superior and LNB writing as per GLP practice. - Experiment observation, dat...
as per shift schedule prepared by respective supervisor or Manager. • Labelling & weighing activity performed as predefined...